SERFAS Energy 0279351650Recalls & reported problems
Stryker Corporation · 50-S Sweep +, Suction Probe, Non-Bendable. · Class 2
All models of SERFAS Energy (17)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 5
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 07613327405811), received between Dec 17, 2020 and Feb 3, 2026 — classified as 5 malfunctions.
The most frequently reported specific device problem is “Break” (2 reports).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- Break2
- Failure to Deliver Energy2
- Material Fragmentation1
Patient problems
- No Clinical Signs, Symptoms or Conditions5
- Insufficient Information2
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 3, 2026Material Fragmentation
IT WAS REPORTED THAT DURING SHOULDER ARTHROSCOPY, THE WHITE TIP OF THE RF DEVICE CHIPPED OFF. THE BROKEN FRAGMENT WAS SUBSEQUENTLY REMOVED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24252859 ↗MalfunctionJan 17, 2025Failure to Deliver Energy; Failure to Deliver Energy
IT WAS REPORTED THAT THE DEVICE HAD INSUFFICIENT / NO ENERGY DELIVERED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21183727 ↗MalfunctionNov 12, 2024Failure to Deliver Energy; Failure to Deliver Energy
IT WAS REPORTED THAT THE DEVICE HAD INSUFFICIENT / NO ENERGY DELIVERED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20668614 ↗MalfunctionJun 30, 2022Break
IT WAS REPORTED THAT THE DEVICE BROKE DURING THE PROCEDURE. ALL PIECES WERE RETRIEVED.
Patient problems: Insufficient Information; No Clinical Signs, Symptoms or Conditions
MAUDE report 14878736 ↗MalfunctionDec 17, 2020Break
IT WAS REPORTED THAT THE TIP BROKE DURING THE PROCEDURE. ALL PIECES WERE RETRIEVED.
Patient problems: Insufficient Information; No Clinical Signs, Symptoms or Conditions
MAUDE report 11032370 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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